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Volumn 13, Issue 5, 2011, Pages 1004-1007

Enantioselective, biocatalytic reduction of 3-substituted cyclopentenones: Application to the asymmetric synthesis of an hNK-1 receptor antagonist

Author keywords

[No Author keywords available]

Indexed keywords

CYCLOPENTANE DERIVATIVE; CYCLOPENTENONE; FUSED HETEROCYCLIC RINGS; NEUROKININ 1 RECEPTOR; PALLADIUM;

EID: 79952169979     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol1030348     Document Type: Article
Times cited : (12)

References (33)
  • 12
    • 0008510209 scopus 로고
    • For an improved synthesis of 8, please refer to the Supporting Information.
    • Zimmerman, H. E.; Pasteris, R. J. J. Org. Chem. 1980, 4864-4876 For an improved synthesis of 8, please refer to the Supporting Information.
    • (1980) J. Org. Chem. , pp. 4864-4876
    • Zimmerman, H.E.1    Pasteris, R.J.2
  • 19
    • 38049073692 scopus 로고    scopus 로고
    • For an excellent review of enzymatic reduction of ketones, see
    • For an excellent review of enzymatic reduction of ketones, see: Moore, J. C.; Pollard, D. J.; Kosjek, B.; Devine, P. N. Acc. Chem. Res. 2007, 1412-1419
    • (2007) Acc. Chem. Res. , pp. 1412-1419
    • Moore, J.C.1    Pollard, D.J.2    Kosjek, B.3    Devine, P.N.4
  • 24
    • 20444497757 scopus 로고    scopus 로고
    • and references cited therein.
    • Muzart, J. Tetrahedron 2005, 5955-6008 and references cited therein.
    • (2005) Tetrahedron , pp. 5955-6008
    • Muzart, J.1
  • 25
    • 79952122554 scopus 로고    scopus 로고
    • Both the acetate and benzoate esters afforded similar yields, but the crystalline naphthoate ester was chosen for isolation purposes.
    • Both the acetate and benzoate esters afforded similar yields, but the crystalline naphthoate ester was chosen for isolation purposes.
  • 33
    • 79952152543 scopus 로고    scopus 로고
    • 3SiH reduction.
    • 3SiH reduction.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.